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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does GILTERITINIB Cause Product use complaint? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product use complaint have been filed in association with GILTERITINIB (Xospata). This represents 0.2% of all adverse event reports for GILTERITINIB.

7
Reports of Product use complaint with GILTERITINIB
0.2%
of all GILTERITINIB reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product use complaint From GILTERITINIB?

Of the 7 reports.

Is Product use complaint Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GILTERITINIB. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does GILTERITINIB Cause?

Acute myeloid leukaemia (366) Febrile neutropenia (346) Off label use (334) Platelet count decreased (327) Pneumonia (302) Myelosuppression (300) Pyrexia (281) Death (206) Product use issue (189) Hepatic function abnormal (181)

What Other Drugs Cause Product use complaint?

TROFINETIDE (472) ENZALUTAMIDE (336) LIFITEGRAST (326) VOXELOTOR (298) CLASCOTERONE (285) NIRMATRELVIR\RITONAVIR (248) ABALOPARATIDE (224) ESTRADIOL (208) MOLNUPIRAVIR (206) ACETAMINOPHEN (202)

Which GILTERITINIB Alternatives Have Lower Product use complaint Risk?

GILTERITINIB vs GIMERACIL\OTERACIL\TEGAFUR GILTERITINIB vs GINKGO GILTERITINIB vs GIVINOSTAT GILTERITINIB vs GIVOSIRAN GILTERITINIB vs GLASDEGIB

Related Pages

GILTERITINIB Full Profile All Product use complaint Reports All Drugs Causing Product use complaint GILTERITINIB Demographics